Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 19:1401418 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041007

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

19:g.1401418C>G
ENST00000447102.5:c.59G>C
ENSP00000403536.2:p.Trp20Ser
ENST00000252288.4:c.59G>C
ENSP00000252288.1:p.Trp20Ser

Variation displays